HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → N-(2-chloro-4-(perfluoropropan-2-yl)-6-(trifluoromethyl)phenyl)-4-iodo-3-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Iodo-3-nitrobenzoic acid | HCID 11208598 | — |
| Reactant | 2-Chloro-4-(perfluoropropan-2-yl)-6-(trifluoromethyl)aniline | HCID 58297418 | — |
| Reactant | 4-Iodo-3-nitrobenzoyl chloride | HCID 58932935 | — |
| Product | N-(2-chloro-4-(perfluoropropan-2-yl)-6-(trifluoromethyl)phenyl)-4-iodo-3-nitrobenzamide | HCID 86654250 | — |
Reaction Steps
According to the method of 1-3 of Example 1, a target compound was prepared from 4-iodo-3-nitrobenzoyl chloride prepared from 4-iodo-3-nitrobenzoic acid and thionyl chloride, and 2-chloro-4-(perfluoropropan-2-yl)-6-(trifluoromethyl)aniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09237745B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-f95d50db96684ba6b950c4d83e7ced37 |
| Source note | uspto-grants-2016_01 |